Patient-Specific Tools And Implants

ABSTRACT

A method for preparing a femoral neck for receiving a neck implant includes resecting a femoral head from a femoral neck of a patient according to a pre-operative patient-specific plan. The method also includes removing only cancellous bone from the femoral neck and proximal femoral bone of the patient using a patient-specific broach. The patient-specific broach has a three-dimensional cutting surface matching as a negative mold a cortical/cancellous bone interface surface of the femoral neck of the patient.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. application Ser. No. 13/041,665filed on Mar. 7, 2011.

The disclosure of the above application is incorporated herein byreference.

INTRODUCTION

The present teachings provide a bone-preserving design for a hipprosthesis. More specifically, the present teachings are directed topatient-specific femoral neck implants and associated tools and methods

SUMMARY

The present teachings provide various methods, tools and implants forpreparing a femoral neck to receive a neck implant.

The present teachings provide a method for preparing a femoral neck forreceiving a neck implant. The method includes obtaining image data of aproximal femoral bone and femoral neck of a patient by a medical imagingmethod and constructing a three-dimensional image model of the proximalfemoral bone and neck of the patient using the image data. The methodfurther includes identifying a three-dimensional cortical boundarysurface at an interface between cortical and cancellous bone of thepatient using the image model. A patient-specific broach having athree-dimensional cutting surface closely matching and complementary tothe cortical boundary surface of the patient using the image model isdesigned and manufactured.

Another method according to the present teachings includes resecting afemoral head from a femoral neck of a patient according to apre-operative patient-specific plan. The method further includesremoving only cancellous bone from the femoral neck and proximal femoralbone of the patient using a patient-specific broach having athree-dimensional cutting surface closely matching and complementary toa cortical/cancellous bone interface surface of the femoral neck of thepatient.

The present teachings provide a femoral neck implant. The femoral neckimplant includes a body for implantation into a femoral neck of apatient. The body has a patient-specific cross-section of variable sizeand shape along a longitudinal axis of the body and a patient-specificthree-dimensional outer surface that closely nests and conformscomplementarily to a cortical boundary surface corresponding to acortical/cancellous bone interface surface of the femoral neck of thespecific patient after removing only the cancellous bone from thefemoral neck. The neck implant can include a neck portion extending fromthe body and configured for coupling with a femoral head implant.

The present teachings provide a femoral neck cutting tool, such as abroach for preparing a femoral neck for a femoral neck implant. Thecutting tool includes a body having a patient-specific cross-section ofvariable size and shape along a longitudinal axis and a patient-specificthree-dimensional outer cutting surface that closely nests and conformscomplementarily to a cortical boundary surface corresponding to acortical/cancellous bone interface surface of a femoral neck of thespecific patient and configured for removing only the cancellous bonefrom the femoral neck of the patient. The cutting tool can include a nonpatient-specific coupling component for engaging a non patent-specificdriver tool.

The present teachings also provide a patient-specific guide forpreparing a femoral neck of a patient for receiving a femoral neckimplant. The patient-specific guide includes a first wall having a firstinner surface with a patient-specific inner bore therethrough, and aperipheral wall extending from the first wall. The first inner surfaceis configured to mate with a resected surface of the femoral neck. Theperipheral wall includes a three-dimensional patient-specific peripheralinner surface configured to mate in only one position with an outerperipheral surface of the femoral neck after resection.

Further areas of applicability of the present teachings will becomeapparent from the description provided hereinafter. It should beunderstood that the description and specific examples are intended forpurposes of illustration only and are not intended to limit the scope ofthe present teachings.

BRIEF DESCRIPTION OF THE DRAWINGS

The present teachings will become more fully understood from thedetailed description and the accompanying drawings, wherein:

FIG. 1 is a perspective view of a patient-specific neck implantaccording to the present teachings;

FIG. 1A is a perspective view of a patient-specific neck implantaccording to the present teachings;

FIG. 2 is an environmental view of the neck implant of FIG. 1;

FIG. 3 is a plan view of the proximal femur showing a resection of thefemoral neck at a plane C;

FIG. 4 is an environmental view showing a patient-specific broach forthe femoral neck implant;

FIG. 5 is a perspective view of a patient-specific broach according tothe present teachings;

FIG. 6 is a plan view of a driver tool for the broach of FIG. 5;

FIG. 7 is a plan view of the driver tool of FIG. 6 coupled to the broachof FIG. 5;

FIG. 8 is a flow chart of a method according to the present teachings;

FIG. 9 is a flow chart of a method according to the present teachings;

FIG. 10 is an exploded environmental view of a patient-specific cuttingguide for a neck implant according to the present teachings; and

FIG. 10A is an environmental view of the cutting guide of FIG. 10.

DESCRIPTION OF VARIOUS EMBODIMENTS

The following description is merely exemplary in nature and is in no wayintended to limit the present teachings, applications, or uses.

The present teachings provide patient-specific tools and implantsdesigned for a conservative hip procedure that conserves a portion offemoral neck of a specific patient.

As described in commonly assigned U.S. application Ser. No. 11/756,057,filed on May 31, 2007, during a preoperative planning, imaging data ofthe relevant anatomy of a patient can be obtained at a medical facilityor doctor's office. The imaging data can include, for example, adetailed scan of a pelvis, hip, knee, ankle or other joint or relevantportion of the patient's anatomy. The imaging data can be obtained usingMRI, CT, X-Ray, ultrasound or any other imaging system. The imaging dataobtained can be used to construct a three-dimensional computer image ofthe joint and prepare an initial pre-operative plan that can includebone or joint preparation, including planning for resections, milling,reaming, broaching, implant selection and fitting, design ofpatient-specific guides, templates, tools and alignment protocol for thesurgical procedure.

Computer modeling for obtaining three-dimensional computer images of therelevant patient's anatomy can be provided by various CAD programsand/or software available from various vendors or developers, such as,for example, from Materialise USA, Plymouth, Mich. The computer modelingprogram can be used to plan a preoperative surgical plan, includingplanning various bone preparation procedures, selecting ordesigning/modifying implants and designing patient-specific guides andtools including patient-specific prosthesis components, andpatient-specific tools, including reaming, broaching, milling, drillingor cutting tools, alignment guides, templates and other patient-specificinstruments.

The pre-operative plan can be stored in any computer storage medium, ina computer file form or any other computer or digital representation.The pre-operative plan, in a digital form associated with interactivesoftware, can be made available via a hard medium, a web-based or mobileor cloud service, a cellular portable device to the surgeon or othermedical practitioner, for review. Using the interactive software, thesurgeon can review the plan, and manipulate the position of images ofvarious implant components relative to an image of the anatomy. Thesurgeon can modify the plan and send it to the manufacturer withrecommendations or changes. The interactive review process can berepeated until a final, approved plan, is sent to the manufacturer.

After the surgical plan is approved by the surgeon, patient-specificimplants and associated tools, including, for example, alignment guides,cutting/milling/reaming/broaching or other tools for the surgicalpreparation of the joint or other anatomy portion of the specificpatient can be designed using a CAD program or other three-dimensionalmodeling software, such as the software provided by Materialise, forexample, according to the surgical plan. Computer instructions of toolpaths for machining the patient-specific tools and/or implants can begenerated and stored in a tool path data file. The tool path data can beprovided as input to a CNC mill or other automated machining system, andthe tools and implants can be machined from polymer, ceramic, metal orother suitable material depending on the use, and sterilized. Thesterilized tools and implants can be shipped to the surgeon or medicalfacility for use during the surgical procedure.

Patient-specific components or tools or portions discussed below aregenerally constructed by a surgical plan approved by the surgeon usingthree-dimensional images of the specific patient's anatomy and made toclosely conform and mate substantially as a negative mold ofcorresponding portions of the patient's anatomy, including bone surfaceswith or without associated soft tissue. MRI scans, for example, allowmodeling of soft tissue, such as articular cartilage, and modeling ofbone portions of different densities, such as inner surfaces matchingcortical and cancellous bone, as discussed below.

The present teachings provide a bone-preserving design for a hipprosthesis and associated tools. The procedure can conserve as much ofthe natural femoral neck 82 of the patient as determined by the surgeondepending on the specific patient by providing a patient-specificfemoral neck implant 100 for supporting a femoral head implant 150, asillustrated in FIGS. 1, 1A and 2.

Referring to FIGS. 1 and 1A, an exemplary patient-specificneck-preserving (“neck implant” for short) 100 can include a body orstem 102 for introduction into the femoral neck 82 as described belowand an optional flange or collar 104 for abutment on a resected surface90 corresponding to a resection plane C of the femoral neck 82 (shown inFIG. 4). A neck implant 100 without the collar 104 is illustrated inFIG. 1A. The neck implant 100 can also include a neck portion 106 whichcan be coupled to a corresponding bore 152 of the femoral head implant150 using a taper-to-taper connection or other type of coupling. Thestem 102 of the neck implant 100 is designed to be patient-specific witha three-dimensional outer surface 108 that is complementary and closelynests and conforms to a cortical/cancellous interface surface 88 wherethe cortical and cancellous bone layers meet (referred to as corticalboundary surface 88 after the cancellous bone is removed) of the femoralneck 82 of the patient only in one position. Identifying thecortical/cancellous interface 88 enables removing only the cancellousbone 84, thereby conserving the hard cortical bone unmodified forengaging the complementary outer surface 108 of the neck implant 100.

Specifically, the neck implant 100 is designed during the pre-operativeplan based on a three-dimensional computer model of the femoral neck 82of the patient as reconstructed from MRI, CT, X-ray or other scans ofthe patient. Referring to FIG. 3, the cortical/cancellous interfacesurface 88 between the cortical bone 86 and the cancellous bone 84 isillustrated after a planar neck resection C is made to separate thenatural femoral head from the portion of the femoral neck 82 to bepreserved below resected surface 90. As can be seen from FIG. 2, theneck implant 100 can be sized and shaped such that it does not extendbeyond the femoral neck 82 into the intramedullary canal of the femoralbone of the patient. The neck implant 100 has a patient-specific depthinto the femoral neck 82 and a patient-specific angle relative to thefemur. Further, because the cortical/cancellous interface surface 88 hasa variable size and shape cross-section, the neck implant 100 has acorresponding variable size and shape cross-section along a longitudinalaxis A of the neck implant 100, which is also specific to each patient.For simplicity, the neck implant 100 is shown in FIG. 1 with a variableoval/elongated and tapering cross-section 103, 103′ (in two differentlocations), although it should be understood that this geometry ismerely exemplary and that the shape and size cross-section 103 along thebody of the neck implant 100 is patient-specific and mirrors thecorresponding shape and size of the cortical/cancellous interfacesurface 88 along the femoral neck 82 of the specific patient. Thecross-section 103 can be oval or elongated and decreasing or tapering insize, but not necessarily linearly. Further, the cross-section 103 maybe and generally is non-symmetric for a specific patient. The neckportion 106 of the neck implant 100 can also be designed to be alignedto a patient-specific articulation direction along a second axis A′which may be at an angle to the longitudinal axis A of the neck implantA, as illustrated in FIG. 2. The neck portion 106 can be also adjustedfor an out-of-plane angle or neck version adjustment.

Referring to FIGS. 3-5, to remove only the spongy cancellous bone 84while preserving substantially all the cortical bone 86, apatient-specific cutting tool, broach or other bone-removing tool 200can be designed during the preoperative plan based on thethree-dimensional computer model of the neck 82 of the patient.Specifically, the broach 200 is designed to have a body 201 with anouter peripheral three-dimensional cutting surface 202 extending from aproximal end surface 204 to a distal end surface 210 of the body 201that closely nests and conforms or matches and is complementary to thecortical/cancellous interface surface 88 only in one position and suchthat only cancellous bone 84 is removed and the cortical boundarysurface 88 is exposed and maintained. Similarly to the neck implant 100,the broach 200 is also a patient-specific and has a variable in shapeand size cross-section 203, which is generally oval/elongated andtapering, but not necessarily linearly, along a longitudinal axis B ofthe broach. Further, the cross-section 203 may be non-symmetric for aspecific patient. The cutting surface 202 is provided with cutting teethand channels or grooves for moving bone chips away from the cavitycreated by the broach 200, as shown in FIG. 4.

Referring to FIGS. 5-7, the patient-specific broach 200 can be coupledto a non-custom driver tool 300 by providing a coupling interfacebetween the proximal end surface 204 of the broach to a distal surface314 of the driver tool 300. The coupling interface can include, forexample, a broach coupling component 220, such as a finger or rod orother protrusion 208 extending from the proximal end surface 204 of thebroach 200 to be received in a corresponding bore or other opening 312defined through the distal surface 314 of the driver tool 300. Thecoupling interface can also include a driver coupling component 320,such as an opening or bore 206 defined through the proximal end surface204 for receiving a distal portion 316 of a retractable bar or rod 310of the driver tool 300. The driver tool 300 can include a body 302, ahandle bar 304, and a proximal flange 318 for impaction. The retractablerod 310 extends along the length of the body 302 and is biased by aproximal spring 308. The rod 310 can be deployed for engaging the broach200 by using a trigger 306 which can be operated by holding with onehand the handle 304 and squeezing the trigger opening 305 with an indexfinger. The broach 200 can be held securely with the driver tool 300, asshown in FIG. 7 and inserted into the femoral neck 82 to remove thecancellous bone 84 and expose the cortical/cancellous interface surface88 for receiving the patient-specific neck implant, as shown in FIGS. 1and 2.

Referring to FIGS. 8 and 9 according to present teachings, image datafrom CT, MRI, X-ray, ultrasound or other scanning of the proximalfemoral bone 80 and femoral neck 82 of a patient are obtained at block400. For modeling the cortical/cancellous interface and identifying thecortical boundary surface 88, the image data may be obtained from MRIscanning or other methods that provide differentiation of bone andtissue layers based on density, composition or other parameters. Athree-dimensional computer image model of the proximal femoral bone 80and femoral neck 82 of the patient can be constructed at block 402 usingcommercially available software, as discussed above. Thethree-dimensional cortical boundary surface 88 can be visible andidentified and confirmed in the image model at block 404 by the surgeon.A neck resection plane can be selected and correspondingpatient-specific femoral alignment guides and/or femoral head resectionguides can be designed, as discussed, for example, in commonly assignedU.S. application Ser. No. 12/893,306, filed Sep. 29, 2010 and U.S.application Ser. No. 12/486,992, filed Jun. 18, 2009 of thecross-reference section, and incorporated herein by reference. Apatient-specific broach 200 having a three-dimensional cutting surface202 matching and complementary to the cortical boundary surface 88 inonly one position can be designed at block 406 using the computer imagemodel of the patient's anatomy. A patient-specific neck implant 100having a three-dimensional surface 108 matching and complementary to thecortical boundary surface 88 in only one position can be designed andmanufactured using the computer image model of the patient's anatomy(block 408). The implant 100 can be impacted into the femoral neck 82and can also be porous coated for bone in-growth. As discussed above,other patient-specific tools, including femoral alignment/cutting guidesto be used for resecting the femoral head, can also be designed andmanufactured using the image model of the patient's anatomy according tothe pre-operative plan.

The patient-specific neck implant 100, patient-specific broach 200 andother custom or non-custom tools are sterilized and shipped to thesurgeon's site. Referring to FIG. 9, intra-operatively, the naturalfemoral head can be resected from the femoral neck 82 at a selectedposition and orientation (plane C in FIG. 4) using, for example,patient-specific alignment guides, patient-specific resection guides,non-custom guides and cutting tools or combinations thereof (block 410).The resection plane C is selected to preserve as much of the naturalfemoral neck 82 as determined in the pre-operative plan. After thenatural femoral head is removed intra-operatively, the patient-specificbroach 200 can be used to remove only the cancellous bone 84 from thefemoral neck 82 and expose the cortical boundary surface 88 of thefemoral neck 82, at block 412. The patient-specific neck implant 100 canthen be implanted, for example, by impaction, in only one position(block 414), and mate with the exposed cortical boundary surface 88, asshown in FIG. 2. A femoral head implant 150 can be coupled to the neckportion 106 of the neck implant 100. The femoral head implant 150 canarticulate with the natural acetabulum or an acetabular implant 151, asdetermined and planned by the surgeon for the specific patient.

Referring to FIGS. 10 and 10A, in some embodiments, a patient-specificmilling or cutting guide 600 can be used with a milling tool 500 toremove the cancellous bone 84 and prepare the femoral neck 82 forreceiving a neck implant 100. The patient-specific milling guide 600 canbe designed during the preoperative plan such that it can be mountedonly in one position on the femoral neck 82, after the femoral head isresected and removed. The milling guide 600 can include a peripheralwall 602 and a first wall 608. The first wall 608 can be substantiallyflat and have a first inner surface 609. The peripheral wall 602 extendsfrom the first wall 608 to a second surface 610 that is opposite thefirst wall 608. The peripheral wall 602 includes a three-dimensionalpatient-specific peripheral inner surface 604 that is configured tonestingly mate and conform only in one position to a remaining (afterresection) three-dimensional outer peripheral surface 83 of the femoralneck 82. The first wall 608 includes a patient-specific bore 606therethrough. The first inner surface 609 is patient-specific andconfigured to mate and conform to the resected surface 90, as shown inFIGS. 10 and 10A. The patient-specific bore 606 is sized and shapedduring the preoperative plan to be patient-specific for guiding acutting portion 502 of a milling or other cutting tool 500 to remove thecancellous bone 84 from the femoral neck 82 to the cortical boundary 88(interface between cortical and cancellous bone) for receiving a neckimplant, such as the patient-specific neck implant 100 discussed above.It is noted that the dimensions the patient-specific milling guide 600,including the depth and size the peripheral inner surface 604, is suchthat the patient-specific milling guide 600 can be mounted over theresected femoral neck 82. In some embodiments, the patient-specificmilling guide can include a split or hinge (not shown) along theinsertion axis or can be formed in two pieces couplable pieces inclamshell fashion, as discussed in commonly assigned U.S. patentapplication Ser. No. 12/486,992, filed Jun. 18, 2009 and incorporatedherein by reference.

The patient-specific broach 200, the patient-specific milling guide 600and the patient-specific implant 100 can be manufactured frombiocompatible materials using machining, rapid manufacturing bystereolithography, laser welding, computer-assisted manufacturing usingnumerical machining or robotic controllers. Patient-specific alignmentand/or resection guides for resecting and removing the femoral head canalso be designed from the image model and manufactured by the abovemethods according to the pre-operative plan for the patient.

The foregoing discussion discloses and describes merely exemplaryarrangements of the present teachings. Furthermore, the mixing andmatching of features, elements and/or functions between variousembodiments is expressly contemplated herein, so that one of ordinaryskill in the art would appreciate from this disclosure that features,elements and/or functions of one embodiment may be incorporated intoanother embodiment as appropriate, unless described otherwise above.Moreover, many modifications may be made to adapt a particular situationor material to the present teachings without departing from theessential scope thereof. One skilled in the art will readily recognizefrom such discussion, and from the accompanying drawings and claims,that various changes, modifications and variations can be made thereinwithout departing from the spirit and scope of the present teachings asdefined in the following claims.

What is claimed is:
 1. A method of preparing a femoral neck forreceiving a femoral neck implant comprising: resecting a femoral headfrom a femoral neck of a patient according to a pre-operativepatient-specific plan; and removing only cancellous bone from thefemoral neck and proximal femoral bone of the patient using apatient-specific broach having a three-dimensional cutting surfacematching as a negative mold a cortical/cancellous bone interface surfaceof the femoral neck of the patient.
 2. The method of claim 1, furthercomprising: coupling a driver tool to the patient-specific broach; andinserting the broach into the femoral neck of the patient.
 3. The methodof claim 2, further comprising: inserting a protrusion extending from aproximal surface of the broach into a bore of a distal surface of thedriver tool; and inserting a distal portion of a retractable rod of thedriver tool into a bore defined through the proximal surface of thebroach to secure the broach to the driver tool.
 4. The method of claim1, further comprising: implanting a patient-specific neck implant havinga three-dimensional outer surface matching as a negative mold thecortical/cancellous bone interface surface of the femoral neck of thepatient after the cancellous bone is removed.
 5. The method of claim 4,further comprising engaging a proximal flange of the neck implant with aresected surface of the femoral neck.
 6. The method of claim 4, furthercomprising coupling a femoral head implant to a neck portion of the neckimplant.
 7. A method of preparing a femoral neck for receiving a femoralneck implant comprising: coupling a driver tool to a patient-specificbroach having a three-dimensional cutting surface matching as a negativemold a three-dimensional cortical/cancellous bone interface surface ofthe femoral neck of the patient; inserting the broach into a resectedfemoral neck of the patient using the driver tool. removing onlycancellous bone from the femoral neck and proximal femoral bone of thepatient using the patient-specific broach; and exposing thethree-dimensional cortical/cancellous bone interface surface afterremoving the cancellous bone.
 8. The method of claim 7, furthercomprising: directing bone chips away from a cavity created by thebroach.
 9. The method of claim 7, further comprising: implanting apatient-specific neck implant having a three-dimensional outer surfacematching as a negative mold the exposed cortical/cancellous boneinterface surface of the femoral neck of the patient after thecancellous bone is removed.
 10. The method of claim 9, furthercomprising engaging a proximal flange of the neck implant to a resectedsurface of the femoral neck.
 11. The method of claim 10, furthercomprising coupling a femoral head implant to a neck portion of the neckimplant.
 12. A method of preparing a femoral neck for receiving afemoral neck implant comprising: resecting a femoral head from a femoralneck of a patient; exposing a corresponding resected surface of thefemoral neck; inserting a patient-specific broach into the resectedfemoral neck of the patient, the patient-specific broach having athree-dimensional cutting surface matching as a negative mold athree-dimensional surface at the interface of the cortical/cancellousbone of the femoral neck of the patient; removing only cancellous bonefrom the femoral neck and proximal femoral bone of the patient using thepatient-specific broach; and exposing the three-dimensionalcortical/cancellous bone interface surface after removing the cancellousbone.
 13. The method of claim 12, further comprising: directing bonechips away from a cavity created by the broach.
 14. The method of claim12, further comprising: coupling a driver tool to the patient-specificbroach.
 15. The method of claim 14, further comprising securing thedriver tool to the broach.
 16. The method of claim 14, furthercomprising inserting a protrusion extending from a proximal surface ofthe broach into a bore of a distal surface of the driver tool.
 17. Themethod of claim 14, further comprising inserting a distal portion of aretractable rod of the driver tool into a bore defined through theproximal surface of the broach.
 18. The method of claim 12, furthercomprising: implanting a patient-specific neck implant having athree-dimensional outer surface matching as a negative mold the exposedcortical/cancellous bone interface surface of the femoral neck of thepatient after the cancellous bone is removed.
 19. The method of claim18, further comprising engaging a proximal flange of the neck implant tothe resected surface of the femoral neck.
 20. The method of claim 19,further comprising coupling a femoral head implant to a neck portion ofthe neck implant.